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S8C28P14-3: This is a hypertrophic, spongiotic and psoriasiform dermatitis which is complicated by angiodermatitis. This association is common; the angiodermatitis tends to mask the nature of the
inflammatory process. Given a choice, in the study of a disseminated cutaneous disease, a biopsy of a site other than the lower extremity will avoid the problem of separating the inflammatory process from the
vaso-proliferative process. The papillary dermis is widened and is edematous, even outside the domain of the lobules of newly formed vessels. To the right, the epidermis, which extends irregularly into the papillary
dermis, shows lichenoid features. There is liquefaction degeneration at the dermal-epidermal interface and, in areas, the extremities of the epithelial columns have pointed extremities. Hypertrophic lichen planus
would have to be considered in the differential diagnosis. Most examples of hypertrophic lichen planus will be encountered on the lower extremities (legs); the hypertrophy is an expression of not only epidermal hyperplasia, but also of a contribution made by an associated angiodermatitis. The epidermis shows focal, mild keratinocytic dysplasia.
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